Clinical trial · Interventional
A Trial of SHR-1701 in Combination With Gemcitabine and Albumin Paclitaxel in Patients With Pancreatic Cancer
A Phase Ib/II Trial of SHR-1701 Combined With Gemcitabine and Albumin Paclitaxel in First-line Treatment of Subjects With Advanced/Metastatic Pancreatic Cancer
NCT04624217CI-TRIAL-00072934completedPhase 1 / Phase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The study is being conducted to evaluate the efficacy, safety and tolerability of SHR-1701 in combination with gemcitabine and albumin paclitaxel in first-line treatment of subjects with advanced/metastatic pancreatic cancer, and determine the RP2D for SHR-1701 in the combined regimen.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Pancreatic Cancer | Malignant Pancreatic Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| SHR-1701 | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- SHR-1701
- description
- SHR-1701 in Combination With Gemcitabine and Albumin Paclitaxel
- interventionNames
- Drug: SHR-1701
Primary outcomes (2)
- measure
- RP2D
- timeFrame
- Up to week 3
- description
- Recommended Phase 2 Dose of SHR-1701
- measure
- ORR
- timeFrame
- Up to approximately 6 months
- description
- Objective Response Rate
Secondary outcomes (6)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 70 Years
Show eligibility criteria text
Inclusion Criteria: * Male or female subjects aged between 18 and 70 years; * Life expectancy ≥ 12 weeks judged by the investigator. * The ECOG performance status was 0-1. * At least 1 measurable lesion conforming to RECIST 1.1 criteria. * In subjects with histologically or cytologically confirmed pancreatic cancer, there was evidence of inoperable locally advanced or distant metastases. * Adequate organ and bone marrow function. * Female subjects of childbearing age must undergo a serum pregnancy test within 7 days before the commencement of the study and the results are negative, and are willing to use a medically approved high potency contraceptive method during the study period and within 3 months after the last administration of the study drug; For male subjects whose partner is a female of childbearing age, they should be surgically sterilized or agree to use an effective method of contraception during the study period and for 3 months after administration of the last study. * Willing to consent and signed the informed consent, and able comply with the planned visit, research treatment, laboratory examination and other test procedures. Exclusion Criteria: * Known allergy to the study drug or any of its excipients; Or had a serious allergic reaction to other monoclonal antibodies. * Previous exposure to drugs/antibodies acting on T cell co-stimulation or checkpoint pathways. * Major surgery within 28 days before the first experimental treatment (biopsy required for diagnosis is permitted). * Subject with central nervous system (CNS) metastases. * Had other active malignant tumors within 5 years before entering the study. Except for basal cell or squamous cell carcinomas, superficial bladder carcinomas, carcinoma in situ of the cervix, ductal carcinoma in situ, and papillary carcinoma of the thyroid, which may be treated locally and have been cured. * Human immunodeficiency virus (HIV) infection or known acquired immunodeficiency syndrome (AIDS), untreated active hepatitis. * The presence of clinically significant acute or chronic pancreatitis. * The presence of other acute or chronic infections of clinically significant significance. * History of allogeneic organ transplantation or allogeneic hematopoietic stem cell transplantation.
References
Publications (1)
- DERIVEDXue R, Wei M, Yuan J, Li Z, Zhou Y, Xue Z, Wu Y, Han H, Zhou J, Yu X, Shen L. A phase 1b/2 study of first-line anti-PD-L1/ TGF-betaRII fusion protein SHR-1701 combined with nab-paclitaxel and gemcitabine for advanced pancreatic ductal adenocarcinoma. Signal Transduct Target Ther. 2025 Dec 20;10(1):415. doi: 10.1038/s41392-025-02530-2. PMID 41422078